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Large-scale production and directed induction of functional dendritic cells ex vivo from serum-free expanded human hematopoietic stem cells
Authors:Shu-Ching Hsu  Li-Cheng Lu  Kuang-Yu Chan  Chien-Hsun Huang  Shih-Lung Cheng  Yung-Shiang Chan  Yu-Shao Yang  Yi-Ting Lai  Chao-Ling Yao
Institution:1. National Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Miaoli County, Taiwan;2. Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;3. Graduate Institute of Cancer Molecular Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan;4. PhD Program in Tissue Engineering and Regenerative Medicine, National Chung Hsing University, Taichung City, Taiwan;5. Department of Medical Research and Development, Chang Bing Show Chwan Memorial Hospital, Changhua County, Taiwan;6. Department of Obstetrics and Gynecology, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan City, Taiwan;7. Department of Chemical Engineering and Materials Science, Yuan Ze University, Chung-Li District, Taoyuan City, Taiwan;8. Department of Internal Medicine, Far Eastern Memorial Hospital, New Taipei City, Taiwan;9. Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, Taiwan
Abstract:BackgroundDendritic cells (DCs) that are derived from hematopoietic stem cells (HSCs) are the most potent antigen-presenting cells and play a pivotal role in initiating the immune response. Hence, large-scale production and direct induction of functional DCs ex vivo from HSCs are crucial to HSC research and clinical potential, such as vaccines for cancer and immune therapy.MethodsIn a previous study, we developed a serum-free HSC expansion system (SF-HSC medium) to expand large numbers of primitive HSCs ex vivo. Herein, a DC induction and expansion medium (DC medium) was proposed to further generate large numbers of functional DCs from serum-free expanded HSCs, which were developed and optimized by factorial design and the steepest ascent method.ResultsThe DC medium is composed of effective basal medium (Iscove's modified Dulbecco's medium IMDM]) and cytokines (2.9 ng/mL stem cell factor SCF], 2.1 ng/mL Flt-3 ligand, 3.6 ng/mL interleukin IL]-1β, 19.3 ng/mL granulocyte-macrophage colony-stimulating factor GM-CSF] and 20.0 ng/mL tumor necrosis factor-α TNF-α]). After 10-day culture in DC medium, the maximum fold expansion for accumulated CD1a+CD11c+ DCs was more than 4000-fold, and the induced DCs were characterized and confirmed by analysis of growth kinetics, surface antigen expression, endocytosis ability, mixed lymphocyte reaction, specific cytokine secretion and lipopolysaccharide stimulation.DiscussionIn conclusion, the combination of DC medium and SF-HSC medium can efficiently induce and expand a large amount of functional DCs from a small scale of HSCs and might be a promising source of DCs for vaccine and immune therapy in the near future.
Keywords:dendritic cells  hematopoietic stem cells  immunotherapy  induction
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